Octreotide (OCT) is a somatostatin analog used for its inhibitory acti
on on multiple GI functions. Although octreotide has numerous clinical
benefits, it has also been shown to inhibit postresectional hyperplas
ia of small bowel and hepatic regeneration. Because octreotide inhibit
s both trophic and anabolic hormones, we hypothesize that the use of o
ctreotide may be detrimental in patients with a recent bowel anastomos
is. To test this hypothesis, 60 male rats were randomized to four equa
l groups following small bowel anastomosis. Group I = control; Group I
I = 10 mg/day of hydrocortisone succinate; Group III = 2.5 mu g/kg/day
octreotide (equivalent of a clinical dose); Group IV = 25 mu g/kg/day
octreotide. Hydrocortisone was used as a negative control because it
is known to have inhibitory effects on small bowel anastomotic healing
. On postoperative Day 7, bursting pressures were measured. Serum T-ki
ninogen levels, as a marker for systemic inflammation, and hydroxyprol
ine content from the anastomotic segments were obtained. These results
indicate that in the rat small bowel model, octreotide did not have a
ny deleterious effect on anastomotic strength, systemic inflammation,
and collagen content, even at high doses. Hydrocortisone, as expected,
showed significant detrimental effects on bursting strength, as well
as decreasing systemic inflammation. These findings have significant c
linical implications, as octreotide could be used without jeopardizing
the intestinal anastomosis.